Processes for producing polyester latexes via solvent-based emulsification

ABSTRACT

A process for making a latex emulsion suitable for use in a toner composition includes contacting at least one amorphous polyester resin with an organic solvent to form a resin mixture, adding a neutralizing agent, and deionized water to the resin mixture, removing the solvent from the formed latex, separating the solvent from water, and recycling the solvent from the resin mixture for utilization in a subsequent phase inversion emulsion process.

TECHNICAL FIELD

The present disclosure relates to processes for producing resinemulsions useful in producing toners. More specifically, more efficientsolvent-based processes are provided for emulsifying amorphous polyesterresins.

BACKGROUND

Numerous processes are within the purview of those skilled in the artfor the preparation of toners. Emulsion aggregation (EA) is one suchmethod. Emulsion aggregation toners may be used in forming print and/orxerographic images. Emulsion aggregation techniques may involve theformation of a polymer emulsion by heating a monomer and undertaking abatch or semi-continuous emulsion polymerization, as disclosed in, forexample, U.S. Pat. No. 5,853,943, the disclosure of which is herebyincorporated by reference in its entirety. Other examples ofemulsion/aggregation/coalescing processes for the preparation of tonersare illustrated in U.S. Pat. Nos. 5,902,710; 5,910,387; 5,916,725;5,919,595; 5,925,488, 5,977,210, 5,994,020, and U.S. Patent ApplicationPublication No. 2008/0107989, the disclosures of each of which arehereby incorporated by reference in their entirety.

Polyester toners have been prepared utilizing amorphous and crystallinepolyester resins as illustrated, for example, in U.S. Patent ApplicationPublication No. 2008/0153027, the disclosure of which is herebyincorporated by reference in its entirety. The incorporation of thesepolyesters into the toner requires that they first be formulated intoemulsions prepared by solvent containing batch processes, for examplesolvent flash emulsification and/or solvent-based phase inversionemulsification (PIE), which is both time and energy-consuming. In bothcases, large amounts of organic solvents, such as ketones or alcohols,have been used to dissolve the resins, which may require subsequentenergy intensive distillation to form the latexes.

Solventless latex emulsions have been formed in either a batch orextrusion process through the addition of a neutralizing solution, asurfactant solution and water to a thermally softened resin asillustrated, for example, in U.S. Patent Application Publication Nos.2009/0208864 and 2009/0246680, the disclosures of each of which arehereby incorporated by reference in their entirety. However, certainamorphous resins may be difficult to process without the use of asolvent in that they do not exhibit a sharp melting point and even at100° C., exhibit substantial viscosities which may work against theformation of emulsions. In addition, certain amorphous resins are moresusceptible to molecular weight degradation in the solvent-free processon account of their composition.

Solvents may be added to amorphous resins to reduce the viscosity andpermit necessary reorientation of chain end, which may stabilize andform particles which lead to the formation of stable latexes. Theadditional process step of distillation to remove the solvent is,however, not desirable, as it adds complexity, energy consumption andcost.

It would be advantageous to provide a more efficient solvent-basedprocess for the preparation of a polymer latex, particularly latexesformed from high molecular weight amorphous resins that degrade throughother emulsification processes, suitable for use in a toner product thathas a high product yield.

SUMMARY

A process of the present disclosure includes the steps of contacting atleast one amorphous polyester resin with an organic solvent; melt mixingthe mixture; contacting the melt mixed mixture with a neutralizingagent; contacting the neutralized mixture with de-ionized water to forman emulsion; recovering the organic solvent from the de-ionized watersolution; and continuously recovering latex particles.

A process of the present disclosure also includes contacting at leastone amorphous polyester resin with an organic solvent to form a resinmixture; melt mixing the mixture; contacting the melt mixed mixture witha neutralizing agent; contacting the neutralized mixture with de-ionizedwater to form an emulsion; recovering the organic solvent from theemulsion; continuously recovering latex particles from the emulsion;contacting the latex particles with an optional colorant, an optionalwax, and a second amorphous polyester resin to form toner particles, andutilizing the recycled organic solvent in a subsequent emulsificationprocess.

Processes are provided which includes contacting at least one amorphouspolyester resin with a recycled organic solvent from a previousemulsification process to form a resin mixture; melt mixing the mixture;contacting the melt mixed mixture with a neutralizing agent; contactingthe neutralized mixture with de-ionized water to form an emulsion;continuously recovering latex particles from the emulsion; andcontacting the latex particles with an optional colorant, an optionalwax, an optional additive, and a second amorphous polyester resin toform toner particles.

BRIEF DESCRIPTION OF DRAWINGS

Various embodiments of the present disclosure will be described hereinbelow with reference to the figures wherein:

FIG. 1 is a graph depicting particle size distribution for the latexproduced in accordance with Example 1 of the present disclosure;

FIG. 2 is a graph depicting particle size distribution for the latexproduced in accordance with Example 2 of the present disclosure;

FIG. 3 is a graph depicting particle size distribution for the latexproduced in accordance with Example 3 of the present disclosure; and

FIG. 4 is a graph depicting particle size distribution for the latexproduced in accordance with Example 4 of the present disclosure.

DETAILED DESCRIPTION

The present disclosure provides solvent based processes for forming highyield polyester latexes which may be utilized in forming a toner.

The addition of at least two solvents, in embodiments methyl ethylketone (MEK) and isopropanol (IPA), to an amorphous polyester resinallows the amorphous polyester resin to be emulsified in a solventprocess. Without the solvents, the amorphous resin does not emulsifyunder the same solvent-free experimental conditions. This is because theamorphous resins exhibit substantial viscosities. Viscous forces actagainst the formation of emulsions as is evident in the solvent basedphase inversion emulsification (PIE) process currently practiced, sincesolvents are added to reduce viscosity and permit the necessaryreorientation of chain ends to stabilize and form particles which leadto the formation of stable latexes without surfactant.

The use of two solvents however makes difficult the recycling of thesolvents and adds greatly to the cost of process. In particularrecycling of the solvent system may be difficult because of the highsolubility of IPA in the water phase.

A recyclable solvent PIE process for use with amorphous resins thatsimplifies the separation and recycling of the solvent to reduce thecost of the process is therefore desirable.

In accordance with the present disclosure, a new formulation and processfor the emulsification of amorphous polyester resins using a singlesolvent system and for recovering and recycling the solvent for asubsequent PIE is provided. In embodiments, the process and formulationtherefore limit the amount of solvent waste generated in the PIE processby at least about 75%.

In embodiments, the present disclosure provides a process which includescontacting at least one amorphous polyester resin with an organicsolvent; melt mixing the mixture; contacting the melt mixed mixture witha neutralizing agent; contacting the neutralized mixture with de-ionizedwater to form an emulsion; recovering the organic solvent from thesolvent/de-ionized water solution; and continuously recovering latexparticles.

In embodiments, the present disclosure provides a process which includescontacting at least one amorphous polyester resin with an organicsolvent to form a resin mixture; melt mixing the mixture; contacting themelt mixed mixture with a neutralizing agent; contacting the neutralizedmixture with de-ionized water to form an oil in water emulsion;recovering the organic solvent from the de-ionized water solution;continuously recovering latex particles; contacting the latex particleswith an optional colorant, an optional wax, and a second amorphouspolyester resin to form a shell over the latex particles, therebyforming toner particles; and utilizing the recycled organic solvent in asubsequent emulsification process.

In embodiments, the present disclosure provides a high yield toner whichincludes at least one amorphous polyester resin; a recycled organicsolvent, wherein the recycled organic solvent is optionally salted out;a neutralizing agent; de-ionized water; and an optional colorant withoptional toner additives.

Resins

Any resin may be utilized in forming a latex emulsion of the presentdisclosure. In embodiments, the resins may be an amorphous resin, acrystalline resin, and/or a combination thereof. In further embodiments,the resin may be a polyester resin, including the resins described inU.S. Pat. Nos. 6,593,049 and 6,756,176, the disclosures of each of whichare hereby incorporated by reference in their entirety. Suitable resinsmay also include a mixture of an amorphous polyester resin and acrystalline polyester resin as described in U.S. Pat. No. 6,830,860, thedisclosure of which is hereby incorporated by reference in its entirety.Suitable resins may include a mixture of high molecular and lowmolecular weight amorphous polyester resins.

In embodiments, the resin may be a polyester resin formed by reacting adiol with a diacid in the presence of an optional catalyst. For forminga crystalline polyester, suitable organic diols include aliphatic diolswith from about 2 to about 36 carbon atoms, such as 1,2-ethanediol,1,3-propanediol, 1,4-butanediol, 1,5-pentanediol,2,2-dimethylpropane-1,3-diol, 1,6-hexanediol, 1,7-heptanediol,1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,12-dodecanediol andthe like including their structural isomers. The aliphatic diol may be,for example, selected in an amount of from about 40 to about 60 molepercent, in embodiments from about 42 to about 55 mole percent, inembodiments from about 45 to about 53 mole percent, and a second diolcan be selected in an amount of from about 0 to about 10 mole percent,in embodiments from about 1 to about 4 mole percent of the resin.

Examples of organic diacids or diesters including vinyl diacids or vinyldiesters selected for the preparation of the crystalline resins includeoxalic acid, succinic acid, glutaric acid, adipic acid, suberic acid,azelaic acid, sebacic acid, fumaric acid, dimethyl fumarate, dimethylitaconate, cis, 1,4-diacetoxy-2-butene, diethyl fumarate, diethylmaleate, phthalic acid, isophthalic acid, terephthalic acid,naphthalene-2,6-dicarboxylic acid, naphthalene-2,7-dicarboxylic acid,cyclohexane dicarboxylic acid, malonic acid and mesaconic acid, adiester or anhydride thereof. The organic diacid may be selected in anamount of, for example, in embodiments from about 40 to about 60 molepercent, in embodiments from about 42 to about 52 mole percent, inembodiments from about 45 to about 50 mole percent, and a second diacidcan be selected in an amount of from about 0 to about 10 mole percent ofthe resin.

Examples of crystalline resins include polyesters, polyamides,polyimides, polyolefins, polyethylene, polybutylene, polyisobutyrate,ethylene-propylene copolymers, ethylene-vinyl acetate copolymers,polypropylene, mixtures thereof, and the like. Specific crystallineresins may be polyester based, such as poly(ethylene-adipate),poly(propylene-adipate), poly(butylene-adipate),poly(pentylene-adipate), poly(hexylene-adipate), poly(octylene-adipate),poly(ethylene-succinate), poly(propylene-succinate),poly(butylene-succinate), poly(pentylene-succinate),poly(hexylene-succinate), poly(octylene-succinate),poly(ethylene-sebacate), poly(propylene-sebacate),poly(butylene-sebacate), poly(pentylene-sebacate),poly(hexylene-sebacate), poly(octylene-sebacate),poly(decylene-sebacate), poly(decylene-decanoate),poly(ethylene-decanoate), poly(ethylene dodecanoate),poly(nonylene-sebacate), poly(nonylene-decanoate),copoly(ethylene-fumarate)-copoly(ethylene-sebacate),copoly(ethylene-fumarate)-copoly(ethylene-decanoate),copoly(ethylene-fumarate)-copoly(ethylene-dodecanoate),copoly(2,2-dimethylpropane-1,3-diol-decanoate)-copoly(nonylene-decanoate),poly(octylene-adipate). Examples of polyamides includepoly(ethylene-adipamide), poly(propylene-adipamide),poly(butylenes-adipamide), poly(pentylene-adipamide),poly(hexylene-adipamide), poly(octylene-adipamide),poly(ethylene-succinimide), and poly(propylene-sebecamide). Examples ofpolyimides include poly(ethylene-adipimide), poly(propylene-adipimide),poly(butylene-adipimide), poly(pentylene-adipimide),poly(hexylene-adipimide), poly(octylene-adipimide),poly(ethylene-succinimide), poly(propylene-succinimide), andpoly(butylene-succinimide).

The crystalline resin may be present, for example, in an amount of fromabout 1 to about 50 percent by weight of the toner components, inembodiments from about 5 to about 35 percent by weight of the tonercomponents. The crystalline resin can possess various melting points of,for example, from about 30° C. to about 120° C., in embodiments fromabout 50° C. to about 90° C. The crystalline resin may have a numberaverage molecular weight (M_(n)), as measured by gel permeationchromatography (GPC) of, for example, from about 1,000 to about 50,000,in embodiments from about 2,000 to about 25,000, and a weight averagemolecular weight (M_(w)) of, for example, from about 2,000 to about100,000, in embodiments from about 3,000 to about 80,000, as determinedby Gel Permeation Chromatography using polystyrene standards. Themolecular weight distribution (M_(w)/M_(n)) of the crystalline resin maybe, for example, from about 2 to about 6, in embodiments from about 3 toabout 4.

Examples of diacids or diesters including vinyl diacids or vinyldiesters utilized for the preparation of amorphous polyesters includedicarboxylic acids or diesters such as terephthalic acid, phthalic acid,isophthalic acid, fumaric acid, trimellitic acid, dimethyl fumarate,dimethyl itaconate, cis, 1,4-diacetoxy-2-butene, diethyl fumarate,diethyl maleate, maleic acid, succinic acid, itaconic acid, succinicacid, succinic anhydride, dodecylsuccinic acid, dodecylsuccinicanhydride, glutaric acid, glutaric anhydride, adipic acid, pimelic acid,suberic acid, azelaic acid, dodecanediacid, dimethyl terephthalate,diethyl terephthalate, dimethylisophthalate, diethylisophthalate,dimethylphthalate, phthalic anhydride, diethylphthalate,dimethylsuccinate, dimethylfumarate, dimethylmaleate, dimethylglutarate,dimethyladipate, dimethyl dodecylsuccinate, and combinations thereof.The organic diacids or diesters may be present, for example, in anamount from about 40 to about 60 mole percent of the resin, inembodiments from about 42 to about 52 mole percent of the resin, inembodiments from about 45 to about 50 mole percent of the resin.

Examples of diols which may be utilized in generating the amorphouspolyester include 1,2-propanediol, 1,3-propanediol, 1,2-butanediol,1,3-butanediol, 1,4-butanediol, pentanediol, hexanediol,2,2-dimethylpropanediol, 2,2,3-trimethylhexanediol, heptanediol,dodecanediol, bis(hydroxyethyl)-bisphenol A,bis(2-hydroxypropyl)-bisphenol A, 1,4-cyclohexanedimethanol,1,3-cyclohexanedimethanol, xylenedimethanol, cyclohexanediol, diethyleneglycol, bis(2-hydroxyethyl) oxide, dipropylene glycol, dibutylene, andcombinations thereof. The amount of organic diols selected can vary, andmay be present, for example, in an amount from about 40 to about 60 molepercent of the resin, in embodiments from about 42 to about 55 molepercent of the resin, in embodiments from about 45 to about 53 molepercent of the resin.

Polycondensation catalysts which may be utilized in forming either thecrystalline or amorphous polyesters include tetraalkyl titanates,dialkyltin oxides such as dibutyltin oxide, tetraalkyltins such asdibutyltin dilaurate, and dialkyltin oxide hydroxides such as butyltinoxide hydroxide, aluminum alkoxides, alkyl zinc, dialkyl zinc, zincoxide, stannous oxide, or combinations thereof. Such catalysts may beutilized in amounts of, for example, from about 0.01 mole percent toabout 5 mole percent based on the starting diacid or diester used togenerate the polyester resin.

In embodiments, as noted above, an unsaturated amorphous polyester resinmay be utilized as a latex resin. Examples of such resins include thosedisclosed in U.S. Pat. No. 6,063,827, the disclosure of which is herebyincorporated by reference in its entirety. Exemplary unsaturatedamorphous polyester resins include, but are not limited to,poly(propoxylated bisphenol co-fumarate), poly(ethoxylated bisphenolco-fumarate), poly(butyloxylated bisphenol co-fumarate),poly(co-propoxylated bisphenol co-ethoxylated bisphenol co-fumarate),poly(1,2-propylene fumarate), poly(propoxylated bisphenol co-maleate),poly(ethoxylated bisphenol co-maleate), poly(butyloxylated bisphenolco-maleate), poly(co-propoxylated bisphenol co-ethoxylated bisphenolco-maleate), poly(1,2-propylene maleate), poly(propoxylated bisphenolco-itaconate), poly(ethoxylated bisphenol co-itaconate),poly(butyloxylated bisphenol co-itaconate), poly(co-propoxylatedbisphenol co-ethoxylated bisphenol co-itaconate), poly(1,2-propyleneitaconate), and combinations thereof.

In embodiments, a suitable polyester resin may be an amorphous polyestersuch as a poly(propoxylated bisphenol A co-fumarate) resin having thefollowing formula (I):

wherein m may be from about 5 to about 1000. Examples of such resins andprocesses for their production include those disclosed in U.S. Pat. No.6,063,827, the disclosure of which is hereby incorporated by referencein its entirety.

An example of a linear propoxylated bisphenol A fumarate resin which maybe utilized as a latex resin is available under the trade name SPARIIfrom Resana S/A Industrias Quimicas, Sao Paulo Brazil. Otherpropoxylated bisphenol A fumarate resins that may be utilized and arecommercially available include GTUF and FPESL-2 from Kao Corporation,Japan, and EM181635 from Reichhold, Research Triangle Park, NorthCarolina, and the like.

Suitable crystalline resins which may be utilized, optionally incombination with an amorphous resin as described above, include thosedisclosed in U.S. Patent Application Publication No. 2006/0222991, thedisclosure of which is hereby incorporated by reference in its entirety.In embodiments, a suitable crystalline resin may include a resin formedof ethylene glycol and a mixture of dodecanedioic acid and fumaric acidco-monomers with the following formula:

wherein b is from about 5 to about 2000 and d is from about 5 to about2000.

For example, in embodiments, a poly(propoxylated bisphenol Aco-fumarate) resin of formula I as described above may be combined witha crystalline resin of formula II to form a latex emulsion.

The amorphous resin may be present, for example, in an amount of fromabout 30 to about 100 percent by weight of the toner components, inembodiments from about 40 to about 95 percent by weight of the tonercomponents. In embodiments, the amorphous resin or combination ofamorphous resins utilized in the latex may have a glass transitiontemperature of from about 30° C. to about 80° C., in embodiments fromabout 35° C. to about 70° C. In further embodiments, the combined resinsutilized in the latex may have a melt viscosity of from about 10 toabout 1,000,000 Pa*S at about 130° C., in embodiments from about 50 toabout 100,000 Pa*S.

One, two, or more resins may be used. In embodiments, where two or moreresins are used, the resins may be in any suitable ratio (e.g., weightratio) such as for instance of from about 1% (first resin)/99% (secondresin) to about 99% (first resin)/1% (second resin), in embodiments fromabout 10% (first resin)/90% (second resin) to about 90% (firstresin)/10% (second resin).

In embodiments, a suitable toner of the present disclosure may include 2amorphous polyester resins and a crystalline polyester resin. The weightratio of the three resins may be from about 29% first amorphousresin/69% second amorphous resin/2% crystalline resin, to about 60%first amorphous resin/20% second amorphous resin/20% crystalline resin.

In embodiments, a suitable toner of the present disclosure may includeat least 2 amorphous polyester resins, a high molecular weight resin anda low molecular weight resin. As used herein, a high molecular weightamorphous resin may have a weight average molecular weight (Mw) of fromabout 35,000 to about 150,000, in embodiments from about 45,000 to about140,000, and a low low molecular weight amorphous resin may have a Mw offrom about 10,000 to about 30,000, in embodiments from about 15,000 toabout 25,000.

The weight ratio of the two resins may be from about 10% first amorphousresin/90% second amorphous resin, to about 90% first amorphous resin/10%second amorphous resin.

In embodiments the resin may possess acid groups which, in embodiments,may be present at the terminal of the resin. Acid groups which may bepresent include carboxylic acid groups, and the like. The number ofcarboxylic acid groups may be controlled by adjusting the materialsutilized to form the resin and reaction conditions.

In embodiments, the resin may be a polyester resin having an acid numberfrom about 2 mg KOH/g of resin to about 200 mg KOH/g of resin, inembodiments from about 5 mg KOH/g of resin to about 50 mg KOH/g ofresin. The acid containing resin may be dissolved in tetrahydrofuransolution. The acid number may be detected by titration with KOH/methanolsolution containing phenolphthalein as the indicator. The acid numbermay then be calculated based on the equivalent amount of KOH/methanolrequired to neutralize all the acid groups on the resin identified asthe end point of the titration.

Solvent

Any suitable organic solvent may be used to dissolve the resin, forexample, alcohols, esters, ethers, ketones, amines, and combinationsthereof, in an amount of, for example, from about 30% by weight to about400% by weight of the resin, in embodiments, from about 40% by weight toabout 250% by weight of the resin, in embodiments, from about 50% byweight to about 100% by weight of the resin.

In embodiments, suitable organic solvents, sometimes referred to herein,in embodiments, as phase inversion agents, include, for example,methanol, ethanol, propanol, isopropanol, butanol, ethyl acetate, methylethyl ketone, and combinations thereof. In embodiments, the organicsolvent may be immiscible in water and may have a boiling point of fromabout 30° C. to about 120° C. In embodiments, the organic solventutilized may be methyl ethyl ketone (MEK).

Neutralizing Agent

In embodiments, the resin may be mixed with a weak base or neutralizingagent. In embodiments, the neutralizing agent may be used to neutralizeacid groups in the resins, so a neutralizing agent herein may also bereferred to as a “basic neutralization agent.” Any suitable basicneutralization reagent may be used in accordance with the presentdisclosure. In embodiments, suitable basic neutralization agents mayinclude both inorganic basic agents and organic basic agents. Suitablebasic agents may include ammonium hydroxide, potassium hydroxide, sodiumhydroxide, sodium carbonate, sodium bicarbonate, lithium hydroxide,potassium carbonate, combinations thereof, and the like. Suitable basicagents may also include monocyclic compounds and polycyclic compoundshaving at least one nitrogen atom, such as, for example, secondaryamines, which include aziridines, azetidines, piperazines, piperidines,pyridines, bipyridines, terpyridines, dihydropyridines, morpholines,N-alkylmorpholines, 1,4-diazabicyclo[2.2.2]octanes,1,8-diazabicycloundecanes, 1,8-diazabicycloundecenes, dimethylatedpentylamines, trimethylated pentylamines, pyrimidines, pyrroles,pyrrolidines, pyrrolidinones, indoles, indolines, indanones,benzindazones, imidazoles, benzimidazoles, imidazolones, imidazolines,oxazoles, isoxazoles, oxazolines, oxadiazoles, thiadiazoles, carbazoles,quinolines, isoquinolines, naphthyridines, triazines, triazoles,tetrazoles, pyrazoles, pyrazolines, and combinations thereof. Inembodiments, the monocyclic and polycyclic compounds may beunsubstituted or substituted at any carbon position on the ring.

In embodiments, an emulsion formed in accordance with the presentdisclosure may also include a small quantity of water, in embodiments,de-ionized water (DIW), in amounts of from about 30% to about 95%, inembodiments, of from about 30% to about 60%, at temperatures that meltor soften the resin, of from about 40° C. to about 120° C., inembodiments from about 60° C. to about 100° C.

The basic agent may be utilized in an amount of from about 0.001% byweight to 50% by weight of the resin, in embodiments from about 0.01% byweight to about 25% by weight of the resin, in embodiments from about0.1% by weight to 5% by weight of the resin. In embodiments, theneutralizing agent may be added in the form of an aqueous solution. Inother embodiments, the neutralizing agent may be added in the form of asolid.

Utilizing the above basic neutralization agent in combination with aresin possessing acid groups, a neutralization ratio of from about 50%to about 300% may be achieved, in embodiments from about 70% to about200%. In embodiments, the neutralization ratio may be calculated as themolar ratio of basic groups provided with the basic neutralizing agentto the acid groups present in the resin multiplied by 100%.

As noted above, the basic neutralization agent may be added to a resinpossessing acid groups. The addition of the basic neutralization agentmay thus raise the pH of an emulsion including a resin possessing acidgroups from about 5 to about 12, in embodiments, from about 6 to about11. The neutralization of the acid groups may, in embodiments, enhanceformation of the emulsion.

Surfactants

In embodiments, the process of the present disclosure may optionallyinclude adding a surfactant, before or during the melt mixing, to theresin at an elevated temperature. In embodiments, the surfactant may beadded prior to melt-mixing the resin at an elevated temperature.

Where utilized, a resin emulsion may include one, two, or moresurfactants. The surfactants may be selected from ionic surfactants andnonionic surfactants. Anionic surfactants and cationic surfactants areencompassed by the term “ionic surfactants.” In embodiments, thesurfactant may be added as a solid or as a solution with a concentrationof from about 5% to about 100% (pure surfactant) by weight, inembodiments, from about 10% to about 95% by weight. In embodiments, thesurfactant may be utilized so that it is present in an amount of fromabout 0.01% to about 20% by weight of the resin, in embodiments, fromabout 0.1% to about 16% by weight of the resin, in other embodiments,from about 1% to about 14% by weight of the resin.

Anionic surfactants which may be utilized include sulfates andsulfonates, sodium dodecylsulfate (SDS), sodium dodecylbenzenesulfonate, sodium dodecylnaphthalene sulfate, dialkyl benzenealkylsulfates and sulfonates, acids such as abitic acid available fromAldrich, NEOGEN R™, NEOGEN SC™ obtained from Daiichi Kogyo Seiyaku,combinations thereof, and the like. Other suitable anionic surfactantsinclude, in embodiments, DOWFAX™ 2A1, an alkyldiphenyloxide disulfonatefrom The Dow Chemical Company, and/or TAYCA POWER BN2060 from TaycaCorporation (Japan), which are branched sodium dodecylbenzenesulfonates. Combinations of these surfactants and any of the foregoinganionic surfactants may be utilized in embodiments.

Examples of the cationic surfactants, which are usually positivelycharged, include, for example, alkylbenzyl dimethyl ammonium chloride,dialkyl benzenealkyl ammonium chloride, lauryl trimethyl ammoniumchloride, alkylbenzyl methyl ammonium chloride, alkyl benzyl dimethylammonium bromide, benzalkonium chloride, cetyl pyridinium bromide, C₁₂,C₁₅, C₁₇ trimethyl ammonium bromides, halide salts of quaternizedpolyoxyethylalkylamines, dodecylbenzyl triethyl ammonium chloride,MIRAPOL™ and ALKAQUATT™, available from Alkaril Chemical Company,SANIZOL™ (benzalkonium chloride), available from Kao Chemicals, and thelike, and mixtures thereof.

Examples of nonionic surfactants that may be utilized for the processesillustrated herein include, for example, polyacrylic acid, methalose,methyl cellulose, ethyl cellulose, propyl cellulose, hydroxy ethylcellulose, carboxy methyl cellulose, polyoxyethylene cetyl ether,polyoxyethylene lauryl ether, polyoxyethylene octyl ether,polyoxyethylene octylphenyl ether, polyoxyethylene oleyl ether,polyoxyethylene sorbitan monolaurate, polyoxyethylene stearyl ether,polyoxyethylene nonylphenyl ether, dialkylphenoxypoly(ethyleneoxy)ethanol, available from Rhone-Poulenc as IGEPAL CA210™,IGEPAL CA-520™, IGEPAL CA-720™, IGEPAL CO-890™, IGEPAL CO-720™, IGEPALCO-290™, IGEPAL CA-210™, ANTAROX 890™ and ANTAROX 897™. Other examplesof suitable nonionic surfactants may include a block copolymer ofpolyethylene oxide and polypropylene oxide, including those commerciallyavailable as SYNPERONIC PE/F, in embodiments SYNPERONIC PE/F 108.Combinations of these surfactants and any of the foregoing surfactantsmay be utilized in embodiments.

Processing

As noted above, the present process includes melt mixing a mixture at anelevated temperature containing at least one amorphous resin, an organicsolvent, optionally a surfactant, and a neutralizing agent, wherein theorganic solvent utilized in the process is recycled for subsequent use,and/or wherein the organic solvent utilized is a recycled organicsolvent from a previous emulsification process, to form a latexemulsion. In embodiments, the resins may be pre-blended prior to meltmixing.

More than one resin may be utilized in forming the latex. As notedabove, the resin may be an amorphous resin, or a combination of anamorphous resin with a crystalline resin. In embodiments, the resin maybe an amorphous resin and the elevated temperature may be a temperatureabove the glass transition temperature of the amorphous resin. Infurther embodiments, the resin may be a mixture of amorphous andcrystalline resins and the temperature may be above the glass transitiontemperature of the mixture. In still further embodiments, the resin maybe a mixture of low and high molecular weight amorphous resins.

Thus, in embodiments, a process of the present disclosure may includecontacting at least one resin with an organic solvent to form a resinmixture, heating the resin mixture to an elevated temperature, stirringthe mixture, adding a neutralizing agent to neutralize the acid groupsof the resin, adding water dropwise into the mixture until phaseinversion occurs to form a phase inversed latex emulsion, distilling thelatex to remove from it a water solvent mixture in the distillate andproducing a high quality latex, separating the solvent from the water inthe distillate, optionally adding salt to the water phase to extractfurther water from the organic phase, and reusing the recovered organicsolvent phase in a second phase inversion emulsification. Inembodiments, a recycled organic solvent, which has optionally beensalted out, is utilized to replace 75 to 100% of the organic solvent inthe PIE process. In the phase inversion process, the amorphous and/orthe combination of at least one amorphous and crystalline polyesterresins may be dissolved in a low boiling organic solvent, which solventis immiscible in water, such as methyl ethyl ketone, or any othersolvent noted hereinabove, at a concentration of from about 1% by weightto about 75% by weight resin in solvent, in embodiments from about 5% byweight to about 60% by weight resin in solvent. The resin mixture isthen heated to a temperature of from about 25° C. to about 90° C., inembodiments from about 30° C. to about 85° C. The heating need not beheld at a constant temperature, but may be varied. For example, theheating may be slowly or incrementally increased until a desiredtemperature is achieved.

In accordance with previous prior art processes, an amorphous polyesterlatex may be obtained using a two solvent PIE process which requiresdispersing and solvent stripping steps. In this process, the amorphouspolyester resin may be dissolved in a combination of two organicsolvents, for example, MEK and IPA, to produce a homogenous organicphase. A fixed amount of base solution (such as ammonium hydroxide) isthen added into this organic phase to neutralize acid end groups on thepolyester chain, followed by the addition of de-ionized water (DIW) toform a uniform dispersion of polyester particles in water through phaseinversion. The organic solvents remain in both the polyester particlesand water phase at this stage. Through vacuum distillation, the solventsare stripped off. The distillate obtained contains a mixture ofMEK/IPA/DIW which results in a challenging co-solvent recovery problem.The separation and recycling of this mixture may be difficult and it maybe costly to dispose of the distillate. In this two-solvent PIE process,a resin to solvent (MEK+IPA) ratio of about 10 to about 7 is utilized.

In accordance with the present disclosure, a single solvent may be usedto form the latex. Table 1 compares the conventional process to thesingle solvent system disclosed herein (referred to herein as a“Recyclable PIE process”).

TABLE 1 Comparison of two formulations and cost Conventional PIERecyclable PIE Process Process PIE Formulation Amorphous 10.0 10.0 Resin(kg) MEK (kg) 5.0 10.0 IPA (kg) 1.0 0.0 Solvent Balance Total Solvent6.0 10.0 Req'd (kg) Recycled 0.0 7.5 Solvent (kg) Total New 6.0 2.5Solvent (kg)

In embodiments, the neutralizing agent which may be utilized in theprocess of the present disclosure includes the agents mentionedhereinabove. In embodiments, the optional surfactant utilized may be anyof the surfactants mentioned hereinabove to ensure that proper resinneutralization occurs and leads to a high quality latex with low coarsecontent.

In embodiments, the surfactant may be added to the one or moreingredients of the resin composition before, during, or aftermelt-mixing. In embodiments, the surfactant may be added before, during,or after the addition of the neutralizing agent. In embodiments, thesurfactant may be added prior to the addition of the neutralizing agent.In embodiments, a surfactant may be added to the pre-blend mixture priorto melt mixing.

The melt-mixing temperature may be from about 30° C. to about 100° C.,in embodiments from about 50° C. to about 90° C., in other embodimentsfrom about 55° C. to about 80° C.

Once the resins, neutralizing agent and optional surfactant are meltmixed, the mixture may then be contacted with water, to form a latexemulsion. Water may be added in order to form a latex with a solidscontent of from about 5% to about 50%, in embodiments, of from about 10%to about 40%. While higher water temperatures may accelerate thedissolution process, latexes can be formed at temperatures as low asroom temperature. In other embodiments, water temperatures may be fromabout 40° C. to about 110° C., in embodiments, from about 50° C. toabout 90° C.

In embodiments, a continuous phase inversed emulsion may be formed.Phase inversion can be accomplished by continuing to add an aqueousalkaline solution or basic agent, optional surfactant and/or watercompositions to create a phase inversed emulsion including a dispersephase including droplets possessing the molten ingredients of the resincomposition, and a continuous phase including the surfactant and/orwater composition.

Melt mixing may be conducted, in embodiments, utilizing any means withinthe purview of those skilled in the art. For example, melt mixing may beconducted in a glass kettle with an anchor blade impeller, an extruder,i.e. a twin screw extruder, a kneader such as a Haake mixer, a batchreactor, or any other device capable of intimately mixing viscousmaterials to create near homogenous mixtures.

Stirring, although not necessary, may be utilized to enhance formationof the latex. Any suitable stirring device may be utilized. Inembodiments, the stirring may be at a speed of from about 10 revolutionsper minute (rpm) to about 5,000 rpm, in embodiments from about 20 rpm toabout 2,000 rpm, in other embodiments from about 50 rpm to about 1,000rpm. The stirring need not be at a constant speed, but may be varied.For example, as the heating of the mixture becomes more uniform, thestirring rate may be increased. In embodiments, a homogenizer (that is,a high shear device), may be utilized to form the phase inversedemulsion, but in other embodiments, the process of the presentdisclosure may take place without the use of a homogenizer. Whereutilized, a homogenizer may operate at a rate of from about 3,000 rpm toabout 10,000 rpm.

Although the point of phase inversion may vary depending on thecomponents of the emulsion, the temperature of heating, the stirringspeed, and the like, phase inversion may occur when the basicneutralization agent, optional surfactant, and/or water has been addedso that the resulting resin is present in an amount from about 5% byweight to about 70% by weight of the emulsion, in embodiments from about20% by weight to about 65% by weight of the emulsion, in otherembodiments from about 30% by weight to about 60% by weight of theemulsion.

Following phase inversion, additional surfactant, water, and/or aqueousalkaline solution may optionally be added to dilute the phase inversedemulsion, although this is not required. Following phase inversion, thephase inversed emulsion may be cooled to room temperature, for examplefrom about 20° C. to about 25° C.

In embodiments, distillation with stirring of the organic solvent may beperformed to provide resin emulsion particles with an average diametersize of, for example, from about 50 nm to about 250 nm, in embodimentsfrom about 120 to about 180 nanometers. As noted above, the distillatefrom the present disclosure can be utilized and/or recycled for use in asubsequent phase inversion emulsification process.

In embodiments, for example, the distillate from the process of thepresent disclosure may contain MEK and water. The organic phase rich inMEK may be separated from the aqueous phase through simple gravityseparation using a static device such as, for example a decantationtank, a dynamic device such as for example a hydrocyclone, or any otherseparation techniques known in the art. In embodiments, the MEK-watermixture separation may be enhanced by a process called salt effectdistillation. In this process, a salt (such as, for example, sodiumchloride) may be added to extract water out of the organic phase andinto the aqueous phase thus decreasing the equilibrium solubility ofwater in the organic phase.

In embodiments, the present disclosure provides a formulation andprocess for a single solvent phase inversion emulsification of anamorphous polyester resin into latex, the recovery of the solvent fromthe latex and the reuse or recycling of the solvent. The process andformulation include the steps of: dissolution of the resin at a certaintemperature in a single solvent (such as MEK), and neutralization ofacid groups by adding an aqueous solution of base to the above resinsolution, and emulsification by adding the preheated or room temperaturede-ionized water to the above mixture, followed by removal of thesolvents by a vacuum distillation stage, separation of the solvent fromthe aqueous phase in the distillate through gravity separation methods,and repeating of the above steps with the recycled solvent.

The desired properties of the amorphous polyester emulsion (i.e.particle size and low residual solvent level) can be achieved byadjusting the solvent and neutralizer concentration and processparameters (i.e. reactor temperature, vacuum, and process time).

The process of the present disclosure for the production of polyesterlatex emulsions using PIE eliminates or minimizes wasted product andfacilitates solvent recycling on account of the immiscibility of thewater and aqueous phase.

The emulsified resin particles in the aqueous medium may have asubmicron size, for example of about 1 μm or less, in embodiments about500 nm or less, such as from about 10 nm to about 500 nm, in embodimentsfrom about 50 nm to about 400 nm, in other embodiments from about 100 nmto about 300 nm, in some embodiments about 200 nm. Adjustments inparticle size can be made by modifying the ratio of water to resin, theneutralization ratio, solvent concentration, and solvent composition.

Particle size distribution of a latex of the present disclosure may befrom about 30 nm to about 300 nm, in embodiments, from about 125 nm toabout 200 nm.

The coarse content of the latex of the present disclosure may be fromabout 0.01% by weight to about 5% by weight, in embodiments, from about0.1% by weight to about 3% by weight. The solids content of the latex ofthe present disclosure may be from about 10% by weight to about 50% byweight, in embodiments, from about 20% by weight to about 40% by weight.

The process of the present disclosure for the production of polyesterlatex emulsions using PIE eliminates or minimizes wasted product andproduces latexes with more efficient solvent stripping, solventrecovery, and permits recycling of the solvent.

The latex emulsions of the present disclosure may then be utilized toproduce particles that are suitable for emulsion aggregation ultra lowmelt processes, using a combination of crystalline and amorphouspolyester resins.

Toner

Once the resin mixture has been contacted with water to form an emulsionand the solvent removed from this mixture as described above, theresulting latex may then be utilized to form a toner by any methodwithin the purview of those skilled in the art. The latex emulsion maybe contacted with a colorant, optionally in a dispersion, and otheradditives to form an ultra low melt toner by a suitable process, inembodiments, an emulsion aggregation and coalescence process.

In embodiments, the optional additional ingredients of a tonercomposition including colorant, wax, and other additives, may be addedbefore, during or after melt mixing the resin to form the latex emulsionof the present disclosure. The additional ingredients may be addedbefore, during or after formation of the latex emulsion. In furtherembodiments, the colorant may be added before the addition of thesurfactant.

Colorants

As the colorant to be added, various known suitable colorants, such asdyes, pigments, mixtures of dyes, mixtures of pigments, mixtures of dyesand pigments, and the like, may be included in the toner. Inembodiments, the colorant may be included in the toner in an amount of,for example, about 0.1 to about 35% by weight of the toner, or fromabout 1 to about 15% by weight of the toner, or from about 3 to about10% by weight of the toner, although the amount of colorant can beoutside of these ranges.

As examples of suitable colorants, mention may be made of carbon blacklike REGAL 330® (Cabot), Carbon Black 5250 and 5750 (ColumbianChemicals), Sunsperse Carbon Black LHD 9303 (Sun Chemicals); magnetites,such as Mobay magnetites MO8029™, MO8060™; Columbian magnetites; MAPICOBLACKS™ and surface treated magnetites; Pfizer magnetites CB4799™,CB5300™, CB5600™, MCX6369™; Bayer magnetites, BAYFERROX 8600™, 8610™;Northern Pigments magnetites, NP-604™, NP-608™; Magnox magnetitesTMB-100™, or TMB-104™; and the like. As colored pigments, there can beselected cyan, magenta, yellow, red, green, brown, blue or mixturesthereof. Generally, cyan, magenta, or yellow pigments or dyes, ormixtures thereof, are used. The pigment or pigments are generally usedas water based pigment dispersions.

In general, suitable colorants may include Paliogen Violet 5100 and 5890(BASF), Normandy Magenta RD-2400 (Paul Uhlrich), Permanent Violet VT2645(Paul Uhlrich), Heliogen Green L8730 (BASF), Argyle Green XP-111-S (PaulUhlrich), Brilliant Green Toner GR 0991 (Paul Uhlrich), Lithol ScarletD3700 (BASF), Toluidine Red (Aldrich), Scarlet for Thermoplast NSD PS PA(Ugine Kuhlmann of Canada), Lithol Rubine Toner (Paul Uhlrich), LitholScarlet 4440 (BASF), NBD 3700 (BASF), Bon Red C (Dominion Color), RoyalBrilliant Red RD-8192 (Paul Uhlrich), Oracet Pink RF (Ciba Geigy),Paliogen Red 3340 and 3871K (BASF), Lithol Fast Scarlet L4300 (BASF),Heliogen Blue D6840, D7080, K7090, K6910 and L7020 (BASF), Sudan Blue OS(BASF), Neopen Blue FF4012 (BASF), PV Fast Blue B2G01 (AmericanHoechst), Irgalite Blue BCA (Ciba Geigy), Paliogen Blue 6470 (BASF),Sudan II, III and IV (Matheson, Coleman, Bell), Sudan Orange (Aldrich),Sudan Orange 220 (BASF), Paliogen Orange 3040 (BASF), Ortho Orange OR2673 (Paul Uhlrich), Paliogen Yellow 152 and 1560 (BASF), Lithol FastYellow 0991K (BASF), Paliotol Yellow 1840 (BASF), Novaperm Yellow FGL(Hoechst), Permanerit Yellow YE 0305 (Paul Uhlrich), Lumogen YellowD0790 (BASF), Sunsperse Yellow YHD 6001 (Sun Chemicals), Suco-Gelb 1250(BASF), Suco-Yellow D1355 (BASF), Suco Fast Yellow D1165, D1355 andD1351 (BASF), Hostaperm Pink E™ (Hoechst), Fanal Pink D4830 (BASF),Cinquasia Magenta™ (DuPont), Paliogen Black L9984 (BASF), Pigment BlackK801 (BASF), Levanyl Black A-SF (Miles, Bayer), combinations of theforegoing, and the like.

Other suitable water based colorant dispersions include thosecommercially available from Clariant, for example, Hostafine Yellow GR,Hostafine Black T and Black TS, Hostafine Blue B2G, Hostafine Rubine F6Band magenta dry pigment such as Toner Magenta 6BVP2213 and Toner MagentaEO2 which may be dispersed in water and/or surfactant prior to use.

Specific examples of pigments include Sunsperse BHD 6011X (Blue 15Type), Sunsperse BHD 9312X (Pigment Blue 15 74160), Sunsperse BHD 6000X(Pigment Blue 15:3 74160), Sunsperse GHD 9600X and GHD 6004X (PigmentGreen 7 74260), Sunsperse QHD 6040X (Pigment Red 122 73915), SunsperseRHD 9668X (Pigment Red 185 12516), Sunsperse RHD 9365X and 9504X(Pigment Red 57 15850:1, Sunsperse YHD 6005X (Pigment Yellow 83 21108),Flexiverse YFD 4249 (Pigment Yellow 17 21105), Sunsperse YHD 6020X and6045X (Pigment Yellow 74 11741), Sunsperse YHD 600X and 9604X (PigmentYellow 14 21095), Flexiverse LFD 4343 and LFD 9736 (Pigment Black 777226), Aquatone, combinations thereof, and the like, as water basedpigment dispersions from Sun Chemicals, Heliogen Blue L6900™, D6840™,D7080™, D7020™, Pylam Oil Blue™, Pylam Oil Yellow™, Pigment Blue 1™available from Paul Uhlich & Company, Inc., Pigment Violet 1™, PigmentRed 48™, Lemon Chrome Yellow DCC 1026™, E. D. Toluidine Red™ and Bon RedC™ available from Dominion Color Corporation, Ltd., Toronto, Ontario,Novaperm Yellow FGL™, and the like. Generally, colorants that can beselected are black, cyan, magenta, or yellow, and mixtures thereof.Examples of magentas are 2,9-dimethyl-substituted quinacridone andanthraquinone dye identified in the Color Index as CI-60710, CIDispersed Red 15, diazo dye identified in the Color Index as CI-26050,CI Solvent Red 19, and the like. Illustrative examples of cyans includecopper tetra(octadecyl sulfonamido) phthalocyanine, x-copperphthalocyanine pigment listed in the Color Index as CI-74160, CI PigmentBlue, Pigment Blue 15:3, and Anthrathrene Blue, identified in the ColorIndex as CI-69810, Special Blue X-2137, and the like. Illustrativeexamples of yellows are diarylide yellow 3,3-dichlorobenzideneacetoacetanilides, a monoazo pigment identified in the Color Index as CI12700, CI Solvent Yellow 16, a nitrophenyl amine sulfonamide identifiedin the Color Index as Foron Yellow SE/GLN, CI Dispersed Yellow 332,5-dimethoxy-4-sulfonanilide phenylazo-4′-chloro-2,5-dimethoxyacetoacetanilide, and Permanent Yellow FGL.

In embodiments, the colorant may include a pigment, a dye, combinationsthereof, carbon black, magnetite, black, cyan, magenta, yellow, red,green, blue, brown, combinations thereof, in an amount sufficient toimpart the desired color to the toner. It is to be understood that otheruseful colorants will become readily apparent based on the presentdisclosures.

In embodiments, a pigment or colorant may be employed in an amount offrom about 1% by weight to about 35% by weight of the toner particles ona solids basis, in other embodiments, from about 5% by weight to about25% by weight. However, amounts outside these ranges can also be used,in embodiments.

Wax

Optionally, a wax may also be combined with the resin and a colorant informing toner particles. The wax may be provided in a wax dispersion,which may include a single type of wax or a mixture of two or moredifferent waxes. A single wax may be added to toner formulations, forexample, to improve particular toner properties, such as toner particleshape, presence and amount of wax on the toner particle surface,charging and/or fusing characteristics, gloss, stripping, offsetproperties, and the like. Alternatively, a combination of waxes can beadded to provide multiple properties to the toner composition.

When included, the wax may be present in an amount of, for example, fromabout 1% by weight to about 25% by weight of the toner particles, inembodiments from about 5% by weight to about 20% by weight of the tonerparticles, although the amount of wax can be outside of these ranges.

When a wax dispersion is used, the wax dispersion may include any of thevarious waxes conventionally used in emulsion aggregation tonercompositions. Waxes that may be selected include waxes having, forexample, an average molecular weight of from about 500 to about 20,000,in embodiments from about 1,000 to about 10,000. Waxes that may be usedinclude, for example, polyolefins such as polyethylene including linearpolyethylene waxes and branched polyethylene waxes, polypropyleneincluding linear polypropylene waxes and branched polypropylene waxes,polyethylene/amide, polyethylenetetrafluoroethylene,polyethylenetetrafluoroethylene/amide, and polybutene waxes such ascommercially available from Allied Chemical and Petrolite Corporation,for example POLYWAX™ polyethylene waxes such as commercially availablefrom Baker Petrolite, wax emulsions available from Michaelman, Inc. andthe Daniels Products Company, EPOLENE N-15™ commercially available fromEastman Chemical Products, Inc., and VISCOL 550-P™, a low weight averagemolecular weight polypropylene available from Sanyo Kasei K. K.;plant-based waxes, such as carnauba wax, rice wax, candelilla wax,sumacs wax, and jojoba oil; animal-based waxes, such as beeswax;mineral-based waxes and petroleum-based waxes, such as montan wax,ozokerite, ceresin, paraffin wax, microcrystalline wax such as waxesderived from distillation of crude oil, silicone waxes, mercapto waxes,polyester waxes, urethane waxes; modified polyolefin waxes (such as acarboxylic acid-terminated polyethylene wax or a carboxylicacid-terminated polypropylene wax); Fischer-Tropsch wax; ester waxesobtained from higher fatty acid and higher alcohol, such as stearylstearate and behenyl behenate; ester waxes obtained from higher fattyacid and monovalent or multivalent lower alcohol, such as butylstearate, propyl oleate, glyceride monostearate, glyceride distearate,and pentaerythritol tetra behenate; ester waxes obtained from higherfatty acid and multivalent alcohol multimers, such as diethyl ene glycolmonostearate, dipropylene glycol distearate, diglyceryl distearate, andtriglyceryl tetrastearate; sorbitan higher fatty acid ester waxes, suchas sorbitan monostearate, and cholesterol higher fatty acid ester waxes,such as cholesteryl stearate. Examples of functionalized waxes that maybe used include, for example, amines, amides, for example AQUA SUPERSLIP6550™, SUPERSLIP 6530™ available from Micro Powder Inc., fluorinatedwaxes, for example POLYFLUO 190™, POLYFLUO 200™, POLYSILK 19™, POLYSILK14™ available from Micro Powder Inc., mixed fluorinated, amide waxes,such as aliphatic polar amide functionalized waxes; aliphatic waxesconsisting of esters of hydroxylated unsaturated fatty acids, forexample MICROSPERSION 19™ also available from Micro Powder Inc., imides,esters, quaternary amines, carboxylic acids or acrylic polymer emulsion,for example JONCRYL 74™, 89™, 130™, 537™, and 538™, all available fromSC Johnson Wax, and chlorinated polypropylenes and polyethylenesavailable from Allied Chemical and Petrolite Corporation and SC Johnsonwax. Mixtures and combinations of the foregoing waxes may also be usedin embodiments. Waxes may be included as, for example, fuser rollrelease agents. In embodiments, the waxes may be crystalline ornon-crystalline.

In embodiments, the wax may be incorporated into the toner in the formof one or more aqueous emulsions or dispersions of solid wax in water,where the solid wax particle size may be in the range of from about 100to about 300 nm.

Toner Preparation

The toner particles may be prepared by any method within the purview ofone skilled in the art. Although embodiments relating to toner particleproduction are described below with respect to emulsion aggregationprocesses, any suitable method of preparing toner particles may be used,including chemical processes, such as suspension and encapsulationprocesses disclosed in U.S. Pat. Nos. 5,290,654 and 5,302,486, thedisclosures of each of which are hereby incorporated by reference intheir entirety. In embodiments, toner compositions and toner particlesmay be prepared by aggregation and coalescence processes in whichsmall-size resin particles are aggregated to the appropriate tonerparticle size and then coalesced to achieve the final toner particleshape and morphology.

In embodiments, toner compositions may be prepared by emulsionaggregation processes, such as a process that includes aggregating amixture of an optional colorant, an optional wax and any other desiredor required additives, and emulsions including the resins describedabove, optionally in surfactants as described above, and then coalescingthe aggregate mixture. A mixture may be prepared by adding a colorantand optionally a wax or other materials, which may also be optionally ina dispersion(s) including a surfactant, to the emulsion, which may be amixture of two or more emulsions containing the resin. The pH of theresulting mixture may be adjusted by an acid such as, for example,acetic acid, nitric acid or the like. In embodiments, the pH of themixture may be adjusted to from about 2 to about 5. Additionally, inembodiments, the mixture may be homogenized. If the mixture ishomogenized, homogenization may be accomplished by mixing at about 600to about 6,000 revolutions per minute. Homogenization may beaccomplished by any suitable means, including, for example, an IKA ULTRATURRAX T50 probe homogenizer.

Following the preparation of the above mixture, an aggregating agent maybe added to the mixture. Any suitable aggregating agent may be utilizedto form a toner. Suitable aggregating agents include, for example,aqueous solutions of a divalent cation or a multivalent cation material.The aggregating agent may be, for example, an inorganic cationicaggregating agent such as polyaluminum halides such as polyaluminumchloride (PAC), or the corresponding bromide, fluoride, or iodide,polyaluminum silicates such as polyaluminum sulfosilicate (PASS), andwater soluble metal salts including aluminum chloride, aluminum nitrite,aluminum sulfate, potassium aluminum sulfate, calcium acetate, calciumchloride, calcium nitrite, calcium oxylate, calcium sulfate, magnesiumacetate, magnesium nitrate, magnesium sulfate, zinc acetate, zincnitrate, zinc sulfate, zinc chloride, zinc bromide, magnesium bromide,copper chloride, copper sulfate, and combinations thereof. Inembodiments, the aggregating agent may be added to the mixture at atemperature that is below the glass transition temperature (Tg) of theresin.

Suitable examples of organic cationic aggregating agents include, forexample, dialkyl benzenealkyl ammonium chloride, lauryl trimethylammonium chloride, alkylbenzyl methyl ammonium chloride, alkyl benzyldimethyl ammonium bromide, benzalkonium chloride, cetyl pyridiniumbromide, C₁₂, C₁₅, C₁₇ trimethyl ammonium bromides, halide salts ofquaternized polyoxyethylalkylamines, dodecylbenzyl triethyl ammoniumchloride, combinations thereof, and the like.

Other suitable aggregating agents also include, but are not limited to,tetraalkyl titinates, dialkyltin oxide, tetraalkyltin oxide hydroxide,dialkyltin oxide hydroxide, aluminum alkoxides, alkyl zinc, dialkylzinc, zinc oxides, stannous oxide, dibutyltin oxide, dibutyltin oxidehydroxide, tetraalkyl tin, combinations thereof, and the like. Where theaggregating agent is a polyion aggregating agent, the agent may have anydesired number of polyion atoms present. For example, in embodiments,suitable polyaluminum compounds have from about 2 to about 13, in otherembodiments, from about 3 to about 8, aluminum ions present in thecompound.

The aggregating agent may be added to the mixture utilized to form atoner in an amount of, for example, from about 0% to about 10% byweight, in embodiments from about 0.2% to about 8% by weight, in otherembodiments from about 0.5% to about 5% by weight, of the resin in themixture. This should provide a sufficient amount of agent foraggregation.

The particles may be permitted to aggregate until a predetermineddesired particle size is obtained. A predetermined desired size refersto the desired particle size to be obtained as determined prior toformation, and the particle size being monitored during the growthprocess until such particle size is reached. Samples may be taken duringthe growth process and analyzed, for example with a Coulter Counter, foraverage particle size. The aggregation thus may proceed by maintainingthe elevated temperature, or slowly raising the temperature to, forexample, from about 40° C. to about 100° C., and holding the mixture atthis temperature for a time of from about 0.5 hours to about 6 hours, inembodiments from about hour 1 to about 5 hours, while maintainingstirring, to provide the aggregated particles. Once the predetermineddesired particle size is reached, then the growth process is halted.

The growth and shaping of the particles following addition of theaggregation agent may be accomplished under any suitable conditions. Forexample, the growth and shaping may be conducted under conditions inwhich aggregation occurs separate from coalescence. For separateaggregation and coalescence stages, the aggregation process may beconducted under shearing conditions at an elevated temperature, forexample of from about 40° C. to about 90° C., in embodiments from about45° C. to about 80° C., which may be below the glass transitiontemperature of the resin as discussed above.

Once the desired final size of the toner particles is achieved, the pHof the mixture may be adjusted with a base to a value of from about 3 toabout 10, and in embodiments from about 5 to about 9. The adjustment ofthe pH may be utilized to freeze, that is to stop, toner growth. Thebase utilized to stop toner growth may include any suitable base suchas, for example, alkali metal hydroxides such as, for example, sodiumhydroxide, potassium hydroxide, ammonium hydroxide, combinationsthereof, and the like. In embodiments, ethylene diamine tetraacetic acid(EDTA) may be added to help adjust the pH to the desired values notedabove.

In embodiments, the final size of the toner particles may be of fromabout 2 μm to about 12 μm, in embodiments of from about 3 μm to about 10μm.

Shell Resin

In embodiments, after aggregation, but prior to coalescence, a resincoating may be applied to the aggregated particles to form a shellthereover. In embodiments, the core may thus include an amorphous resinand/or a crystalline resin, as described above. Any resin describedabove may be utilized as the shell. In embodiments, a polyesteramorphous resin latex as described above may be included in the shell.In embodiments, the polyester amorphous resin latex described above maybe combined with a different resin, and then added to the particles as aresin coating to form a shell.

In embodiments, resins which may be utilized to form a shell include,but are not limited to, a crystalline resin latex described above,and/or the amorphous resins described above. In embodiments, anamorphous resin which may be utilized to form a shell in accordance withthe present disclosure includes an amorphous polyester, optionally incombination with a crystalline polyester resin latex described above.Multiple resins may be utilized in any suitable amounts. In embodiments,a first amorphous polyester resin, for example an amorphous resin offormula I above, may be present in an amount of from about 20 percent byweight to about 100 percent by weight of the total shell resin, inembodiments from about 30 percent by weight to about 90 percent byweight of the total shell resin. Thus, in embodiments, a second resinmay be present in the shell resin in an amount of from about 0 percentby weight to about 80 percent by weight of the total shell resin, inembodiments from about 10 percent by weight to about 70 percent byweight of the shell resin.

The shell resin may be applied to the aggregated particles by any methodwithin the purview of those skilled in the art. In embodiments, theresins utilized to form the shell may be in an emulsion including anysurfactant described above. The emulsion possessing the resins,optionally the solvent based amorphous polyester resin latex neutralizedwith NaOH described above, may be combined with the aggregated particlesdescribed above so that the shell forms over the aggregated particles.

The formation of the shell over the aggregated particles may occur whileheating to a temperature of from about 30° C. to about 80° C., inembodiments from about 35° C. to about 70° C. The formation of the shellmay take place for a period of time of from about 5 minutes to about 10hours, in embodiments from about 10 minutes to about 5 hours.

The shell may be present in an amount of from about 10 percent by weightto about 40 percent by weight of the latex particles, in embodimentsfrom about 20 percent by weight to about 35 percent by weight of thelatex particles.

Coalescence

Following aggregation to the desired particle size and application ofany optional shell, the particles may then be coalesced to the desiredfinal shape, the coalescence being achieved by, for example, heating themixture to a temperature of from about 45° C. to about 100° C., inembodiments from about 55° C. to about 99° C., which may be at or abovethe glass transition temperature of the resins utilized to form thetoner particles, and/or reducing the stirring, for example to from about1000 rpm to about 100 rpm, in embodiments from about 800 rpm to about200 rpm. Coalescence may be accomplished over a period of from about0.01 to about 9 hours, in embodiments from about 0.1 to about 4 hours.

After aggregation and/or coalescence, the mixture may be cooled to roomtemperature, such as from about 20° C. to about 25° C. The cooling maybe rapid or slow, as desired. A suitable cooling method may includeintroducing cold water to a jacket around the reactor. After cooling,the toner particles may be optionally washed with water, and then dried.Drying may be accomplished by any suitable method for drying including,for example, freeze-drying.

Additives

In embodiments, the toner particles may also contain other optionaladditives, as desired or required. For example, the toner may includepositive or negative charge control agents, for example in an amount offrom about 0.1 to about 10% by weight of the toner, in embodiments fromabout 1 to about 3% by weight of the toner. Examples of suitable chargecontrol agents include quaternary ammonium compounds inclusive of alkylpyridinium halides; bisulfates; alkyl pyridinium compounds, includingthose disclosed in U.S. Pat. No. 4,298,672, the disclosure of which ishereby incorporated by reference in its entirety; organic sulfate andsulfonate compositions, including those disclosed in U.S. Pat. No.4,338,390, the disclosure of which is hereby incorporated by referencein its entirety; cetyl pyridinium tetrafluoroborates; distearyl dimethylammonium methyl sulfate; aluminum salts such as BONTRON E84™ or E88™(Orient Chemical Industries, Ltd.); combinations thereof, and the like.

There can also be blended with the toner particles external additiveparticles after formation including flow aid additives, which additivesmay be present on the surface of the toner particles. Examples of theseadditives include metal oxides such as titanium oxide, silicon oxide,aluminum oxides, cerium oxides, tin oxide, mixtures thereof, and thelike; colloidal and amorphous silicas, such as AEROSIL®, metal salts andmetal salts of fatty acids inclusive of zinc stearate, calcium stearate,or long chain alcohols such as UNILIN 700, and mixtures thereof.

In general, silica may be applied to the toner surface for toner flow,tribo enhancement, admix control, improved development and transferstability, and higher toner blocking temperature. TiO₂ may be appliedfor improved relative humidity (RH) stability, tribo control andimproved development and transfer stability. Zinc stearate, calciumstearate and/or magnesium stearate may optionally also be used as anexternal additive for providing lubricating properties, developerconductivity, tribo enhancement, enabling higher toner charge and chargestability by increasing the number of contacts between toner and carrierparticles. In embodiments, a commercially available zinc stearate knownas Zinc Stearate L, obtained from Ferro Corporation, may be used. Theexternal surface additives may be used with or without a coating.

Each of these external additives may be present in an amount of fromabout 0.1% by weight to about 5% by weight of the toner, in embodimentsof from about 0.25% by weight to about 3% by weight of the toner,although the amount of additives can be outside of these ranges. Inembodiments, the toners may include, for example, from about 0.1% byweight to about 5% by weight titania, from about 0.1% by weight to about8% by weight silica, and from about 0.1% by weight to about 4% by weightzinc stearate.

Suitable additives include those disclosed in U.S. Pat. Nos. 3,590,000,3,800,588, and 6,214,507, the disclosures of each of which are herebyincorporated by reference in their entirety.

The following Examples are being submitted to illustrate embodiments ofthe present disclosure. These Examples are intended to be illustrativeonly and are not intended to limit the scope of the present disclosure.Also, parts and percentages are by weight unless otherwise indicated. Asused herein, “room temperature” refers to a temperature of from about20° C. to about 25° C.

EXAMPLES Example 1

Solvent-based emulsification of an amorphous polyester resin. A 1 literglass kettle was charged with about 200 grams of methyl ethyl ketone(MEK) and about 200 grams of a poly(co-propoxylated bisphenolco-ethoxylated bisphenol co-terephtalate) amorphous polyester resin withan acid value (AV) of about 14.7. The ratio of resin to MEK was about1:1. The glass kettle was placed inside a water bath set at about 48° C.with its cover on, a gasket, a condenser, and an anchor blade impellerfor stirring.

The resin was heated to about 60° C. with stirring at about 60 rpm. Themixture was left to stir for about 30 minutes. Once the resin wasmelted/dissolved, the bath temperature was decreased to about 43° C. andabout 6.68 grams of 10% NH₄OH solution (calculated as 10% NH₃) was addedto the mixture drop-wise with a disposable pipette through a rubberstopper during a period of about 2 minutes.

The mixture was left to stir for about 15 minutes. Thereafter, about 600grams of de-ionized water (DIW) at room temperature was pumped into thekettle at a flow rate of about 4.4 grams/minute. The emulsio_(n)produced had a particle size of about 145.5 nm (see FIG. 1) as measuredusing a Nanotrac particle size analyzer. The emulsion/solvent solutionwas then discharged from the 1 liter kettle into a 1 liter round bottomflask and attached to a Rotavapor R-210 unit to strip off the solventusing heat at about 70° C. and vacuum with a pressure of from about 150torr to about 500 Torr.

The following three examples utilized recycled MEK from the originalphase inversion emulsification obtained in this Example 1. Thesolvent/water solution stripped with the Rotavapor unit was separatedusing a separatory funnel. This organic/solvent phase was used to makethe following Example 2.

Example 2

Solvent-based emulsification of an amorphous polyester resin withnon-salted out recycled MEK of Example 1. About 2 grams of a linearamorphous resin and about 2 grams of the non-salted out recycled MEK ofExample 1 were added to a small glass vial at a ratio of about 1:1. Thevial was heated in a water bath at about 70° C. until the resin/solventmixture completely dissolved (about 10 minutes). Once dissolved, about0.06 grams of a 10% ammonium hydroxide solution was added drop wise withhand shaking for about 1 to about 2 minutes. Thereafter, about 6 gramsof DIW was added to the vial with hand shaking for about 2 to about 3minutes. Final emulsion particle size was about 176.5 nanometers with astandard deviation of about 0.0481, as illustrated in FIG. 2.

An amount of sodium chloride sufficient to change the MEK's miscibilityin water, to force more MEK to separate out (about 10 grams to about 20grams), was added to the remaining solvent/water solution still in theseparatory flask. This organic/solvent phase was determined to containabout 94.8% MEK by a gas chromatograph (GC); as compared withtheoretical values of water content in MEK at about 10%. Thus, bysalting-out the organic/solvent phase, MEK recovery was increased byabout 4.8%. This salted-out organic/solvent phase was then used in thefollowing two examples.

Example 3

Solvent-based emulsification of an amorphous polyester resin with saltedout recycled MEK recovered in Example 2. About 2 grams of a linearamorphous resin and about 2 grams of the salted out recycled MEK ofExample 2 were added to a small glass vial at a ratio of about 1:1. Thevial was heated in a water bath at about 75° C. until the resin/solventmixture completely dissolved (about 10 minutes). Once dissolved, about0.06 grams of a 10% ammonium hydroxide solution was added drop wise withhand shaking for about 1 to about 2 minutes. Thereafter, about 6 gramsof DIW was added to the vial with hand shaking for about 2 to about 3minutes. Final emulsion particle size was about 148.2 nanometers with astandard deviation of about 0.0434, as illustrated in FIG. 3.

Example 4

Solvent-based emulsification of an amorphous polyester resin with saltedout recycled MEK recovered in Example 2. About 2 grams of a branchedamorphous resin and about 3 grams of the salted out recycled MEK ofExample 2 were added to a small glass vial at a ratio of about 1:1.5.The vial was heated in a water bath at about 75° C. until theresin/solvent mixture completely dissolved (about 10 minutes). Oncedissolved, about 0.07 grams of a 10% ammonium hydroxide solution wasadded drop wise with hand shaking for about 1 to about 2 minutes.Thereafter, about 6 grams of DIW was added to the vial with hand shakingfor about 2 to about 3 minutes. Final emulsion particle size was about143.6 nanometers with a standard deviation of about 0.0578, asillustrated in FIG. 4.

It will be appreciated that variations of the above-disclosed and otherfeatures and functions, or alternatives thereof, may be desirablycombined into many other different systems or applications. Also thatvarious presently unforeseen or unanticipated alternatives,modifications, variations or improvements therein may be subsequentlymade by those skilled in the art which are also intended to beencompassed by the following claims. Unless specifically recited in aclaim, steps or components of claims should not be implied or importedfrom the specification or any other claims as to any particular order,number, position, size, shape, angle, color, or material.

1. A process comprising: contacting at least one amorphous polyesterresin with an organic solvent to form a resin mixture; melt mixing themixture; contacting the melt mixed mixture with a neutralizing agent;contacting the neutralized mixture with de-ionized water to form anemulsion; recovering the organic solvent from the emulsion; continuouslyrecovering latex particles from the emulsion; contacting the latexparticles with an optional colorant, an optional wax, and a secondamorphous polyester resin to form toner particles, and utilizing therecycled organic solvent in a subsequent emulsification process.
 2. Aprocess according to claim 1, wherein the organic solvent is selectedfrom the group consisting of esters, ethers, ketones, amines, andcombinations thereof, in an amount of from about 30% by weight to about400% by weight of the polyester resin.
 3. A process according to claim1, wherein the neutralizing agent is added in the form of an aqueoussolution selected from the group consisting of ammonium hydroxide,potassium hydroxide, sodium hydroxide, sodium carbonate, sodiumbicarbonate, lithium hydroxide, potassium carbonate, organoamines, andcombinations thereof, and raises the pH of the resin mixture to fromabout 5 to about
 12. 4. A process according to claim 1, wherein the atleast one amorphous polyester resin is utilized in amounts of from about30 weight % to about 100 weight % of the resin mixture.
 5. A processaccording to claim 1, wherein the second amorphous polyester resin formsa shell over the latex particles and is present in an amount of fromabout 10% by weight to about 40% by weight of the particles.
 6. Aprocess according to claim 1, wherein the latex particles have a solidscontent of from about 10% to about 50%, and wherein the latex particleshave a particle size of from about 30 nm to about 300 nm.
 7. A processaccording to claim 1, wherein said utilizing comprises: contacting atleast one amorphous polyester resin with said recycled organic solventto form a resin mixture; melt mixing the mixture; contacting the meltmixed mixture with a neutralizing agent; contacting the neutralizedmixture with de-ionized water to form an emulsion; continuouslyrecovering latex particles from the emulsion; and contacting the latexparticles with an optional colorant, an optional wax, an optionaladditive, and a second amorphous polyester resin to form tonerparticles.
 8. A process according to claim 7, wherein the recycledorganic solvent is selected from the group consisting of esters, ethers,ketones, amines, and combinations thereof, in an amount of from about30% by weight to about 400% by weight of the polyester resin.
 9. Aprocess according to claim 7, wherein the neutralizing agent is added inthe form of an aqueous solution selected from the group consisting ofammonium hydroxide, potassium hydroxide, sodium hydroxide, sodiumcarbonate, sodium bicarbonate, lithium hydroxide, potassium carbonate,organoamines, and combinations thereof, and raises the pH of the resinmixture to from about 5 to about
 12. 10. A process according to claim 7,wherein the at least one amorphous polyester resin is utilized inamounts of from about 30 weight % to about 100 weight %.
 11. A processaccording to claim 7, wherein the colorant is selected from the groupconsisting of dyes, pigments, mixtures of dyes, mixtures of pigments,mixtures of dyes and pigments, and the like, and is present in amountsof from about 0.1% by weight to about 35% by weight of the toner; andwherein the additives are selected from the group consisting of titaniumoxide, silicon oxide, aluminum oxides, cerium oxides, tin oxide,colloidal and amorphous silicas, zinc stearate, calcium stearate, alkylpyridinium halides, bisulfates, alkyl pyridinium compounds, organicsulfates, organic sulfonates, cetyl pyridinium tetrafluoroborates,distearyl dimethyl ammonium methyl sulfate, aluminum salts, andcombinations thereof.
 12. A process according to claim 7, wherein thetoner particles have a size of from about 2 um to about 12 um.